Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
  • C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
  • A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
  • C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems

Definitions

• the present invention relates to novel dibenzofuran derivatives, fungicides containing these compounds and a method of controlling fungi by means of these active ingredients.
• tetramethylthiuram disulfide as a fungicide has been disclosed in Chem. Week 111 (1972), 39.
• Other fungicides which are no less powerful than tetramethylthiuram disulfide against phytopathogenic fungi eg. Botrytis cinerea, have also been disclosed eg. 2-aminobenzimidazolyl carbamate (R.
• Suitable substituents R 1 , R 2 and R 3 in formula I include halogen, such as fluorine, chlorine, bromine and iodine, nitro, cyano and unsubstituted or halogen-substituted alkyl or alkoxy of 1 to 4 carbon atoms, such as methyl, ethyl, isopropyl, tert.-butyl, methoxy, ethoxy, trifluoromethyl, difluoromethoxy and tetrafluoroethoxy.
• halogen such as fluorine, chlorine, bromine and iodine
• methyl, ethyl, isopropyl, tert.-butyl methoxy, ethoxy, trifluoromethyl, difluoromethoxy and tetrafluoroethoxy
• A.sup. ⁇ in formula I is quinuclidinium or pyrrolizidinium, or --N.sup. ⁇ R 4 R 5 R 6 .
• R 4 , R 5 and R 6 in this formula are alkyl, alkenyl or alkynyl of not more than 6 carbon atoms, preferably of not more than 4 carbon atoms, which may be substituted by halogen, such as fluorine, chlorine or bromine, or by alkoxy of 1 to 4 carbon atoms, cyano or dialkylamino, where alkyl is of 1 to 4 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, n-pentyl, isopentyl, n-hexyl, allyl, but-2-enyl, 4-chloro-but-2-enyl, propargyl, trifluoromethyl, 2-chloroethyl and 2-bro
• R 5 and R 6 can also form an alkylene group which, together with the quaternary nitrogen or which R 5 and R 6 are substituents, form a 5-, 6- or 7-membered heterocyclic ring which has from 1 to 3 hetero-atoms in the ring, for example a pyrrolidinium, piperidinium, hexamethyleneiminium, morpholinium or thiomorpholinium which is substituted by R 4 on the quaternary nitrogen. These rings may be substituted by methyl or ethyl.
• Y.sup. ⁇ can be any desired anion from a non-phytotoxic acid, for example methylsulfonate, p-dodecylbenzenesulfonate, sulfate, methosulfate, nitrate, phosphate, iodide and especially chloride and bromide.
• R 1 is halogen, such as fluorine, chlorine or bromine, straight-chain or branched alkyl or alkoxy of 1 to 4 carbon atoms, such as methyl, ethyl, isopropyl, tert.-butyl, methoxy or ethoxy, nitro or trifluoromethyl
• p and q are 0, n is 1, 2 or 3
• X is oxygen
• m is 2, 3 or 4
• A.sup. ⁇ is -N.sup. ⁇ R 4 R 5 R 6 and Y.sup. ⁇ is the anion of any desired non-phytotoxic acid HY are preferred.
• R 4 , R 5 and R 6 can be identical or different and each independently of one another is straight-chain or branched unsubstituted or halogen-substituted alkyl of 1 to 5 carbon atoms, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, n-pentyl, isopentyl, 2-chloroethyl, 3-chloropropyl, 2-bromoethyl, 3-bromopropyl or 4-bromobutyl, alkenyl of 3 or 4 carbon atoms, such as allyl or but-2-enyl, or cycloalkyl of 3 to 6 carbon atoms, such as cyclopropyl or cyclohexyl.
• alkenyl of 3 or 4 carbon atoms such as allyl or but-2-enyl
• cycloalkyl of 3 to 6 carbon atoms such as cycl
• R 4 is benzyl which is unsubstituted or substituted by fluorine, chlorine, bromine, trifluoromethyl, nitro or alkyl of 1 to 4 carbon atoms, such as benzyl, 2-fluorobenzyl, 4-fluorobenzyl, 2-chlorobenzyl, 4-chlorobenzyl, 3-bromobenzyl, 4-bromobenzyl, 3-trifluoromethylbenzyl, 4-trifluoromethylbenzyl, 2-methylbenzyl, 3-methylbenzyl, 4-methylbenzyl, 4-tert.-butylbenzyl, 4-nitrobenzyl, 2,4-dichlorobenzyl, 3,4-nitrobenzyl, 2,4-dimethylbenzyl or 3,4-dimethylbenzyl, and R 5 together with R 6 is part of a 5-, 6- or 7-membered heterocyclic ring which has from 1 to 3 heteroatoms and may be substituted by methyl or ethyl
• dibenzofuran derivatives of the formula I are N-methyl-N-2-(7-bromodibenzofuran-3-oxy)-ethylpyrrolidinium bromide, N-methyl-N-2-(7-bromodibenzofuran-3-oxy)-ethylpiperidinium bromide, N-allyl-N-2-(7-bromodibenzofuran-3-oxy)-ethyl-(2',6'-dimethylmorpholinium) bromide, N-benzyl-N-2-(7-bromodibenzofuran-3-oxy)-ethylpyrrolidinium bromide, N-benzyl-N-2-(7-bromodibenzofuran-3-oxy)-ethylpiperidinium chloride, N-benzyl-N-4-(7-bromodibenzofuran-3-oxy)-butylpiperidinium chloride, N-methyl-N-4-(7-fluorodibenzofuran-3-
• the dibenzofuran derivatives of the formula I are obtained by reacting
• Reactions (a) and (b) are carried out in the presence or absence of a solvent or diluent at from 20° to 150° C., preferably from 30° to 140° C.
• a solvent or diluent at from 20° to 150° C., preferably from 30° to 140° C.
• the starting substance of the formula II is reacted with a 2-fold to 10-fold molar excess of the amine of the formula A.
• solvents or diluents which are inert toward the reactants are aliphatic or aromatic hydrocarbons or halohydrocarbons, such as pentane, cyclohexane, benzene, toluene, xylene, chlorobenzene and the dichlorobenzenes, aliphatic ketones, such as acetone, methyl ethyl ketone, diethyl ketone and cyclopentanone, ethers, such as diethyl ether, dimethoxyethane, tetrahydrofuran and dioxane, esters, such as ethyl acetate, nitriles, such as acetonitrile, and amides, such as dimethylformamide, dimethylacetamide and N-methylpyrrolidone, and mixtures of these solvents.
• aliphatic or aromatic hydrocarbons or halohydrocarbons such as pentane, cyclohexan
• the starting substances of the formula II can be easily prepared by a conventional process, for example by etherifying a dibenzofuran-3ol or a dibenzofuran-3-thiol with an aliphatic dihalide, such as 1,2-dibromoethane, 1,3-dichloropropane, 1-chloro-3-bromopropane, 1,3-dibromopropane, 1-chloro-4-bromobutane or 1,4-dibromobutane, preferably in boiling methyl ethyl ketone, diethyl ketone or cyclopentanone in the presence of not less than an equivalent amount of sodium carbonate or potassium carbonate (Houben-Weyl, Methoden der Organischen Chemie, Volume 6/3, pages 54-59, Georg Thieme-Verlag, Stuttgart, 1965).
• an aliphatic dihalide such as 1,2-dibromoethane, 1,3-dichloropropane, 1-chloro-3-
• a dibenzofuran-3-oxyalkanol can be reacted with thionyl chloride or with phosphorus tribromide to give a compound of the formula II (Rec. Trav. Chim. 76 (1957), 129-146).
• tertiary amines of the formula A which can be used are trimethylamine, triethylamine, tripropylamine, methyl-diethylamine, methyl-dipropylamine, tributylamine, tripentylamine, 1,2-bis-(dimethylamino)-cyclohexane, N,N-dimethyl-N-cyclododecylamine, N,N-dimethyl-N-cyclohexylamine, N,N-dimethyl-N-benzylamine, N-methylpyrrolidine, N-ethylpyrrolidine, N-allylpyrrolidine, N-propylpyrrolidine, N-butylpyrrolidine, N-methylpiperidine, N-2-dimethylpiperidine, N-3-dimethylpiperidine, N,N-dimethylpiperidine, N-2,4-trimethylpiperidine, N-3,5-trimethylpiperidine, N-2,5-trimethylpiperidine,
• the tertiary amines of the formula III can be prepared by a conventional process, for example in accordance with the equation ##STR5## by alkylating a secondary amine of the formula HNR 5 R 6 , where R 5 and R 6 have the above meanings, with a compound of the formula II.
• the reaction conditions here correspond to those for reaction (a).
• the acid HY formed in the reaction can easily be removed, for example by treating the reaction mixture with an aqueous alkali metal hydroxide solution.
• Suitable amines of the formula HNR 5 R 6 are dimethylamine, dipropylamine, diisopropylamine, diallylamine, dibutylamine, diisobutylamine, N-methylbenzylamine, pyrrolidine, piperidine, 2-methylpiperidine, 3-methylpiperidine, 4-methylpiperidine, 2,4-dimethylpiperidine, 3,5-dimethylpiperidine, 2,6-dimethylpiperidine, 2-ethylpiperidine, N-ethylbenzylamine, N-butylbenzylamine, morpholine, 2-methylmorpholine, 3-methylmorpholine, 2,6-dimethylmorpholine, 2,5-dimethylmorpholine, 2,6-dimethylthiomorpholine and hexamethyleneimine.
• Examples of compounds of the formula IV which can be used are methyl chloride, methyl bromide, methyl iodide, dimethyl sulfate, ethyl chloride, ethyl bromide, ethyl iodide, diethyl sulfate, dibromoethane, 2-methoxyethyl bromide, propyl bromide, propyl iodide, 1-chloro-3-bromopropane, 1,3-dibromopropane, isopropyl bromide, allyl chloride, allyl bromide, n-butyl bromide, butyl chloride, 1,4-dibromobutane, 1,4-dichlorobutane, propargyl chloride, propargyl bromide, 1-bromobut-2-ene, 1,4-dichlorobut-2-ene, benzyl chloride, benzyl bromide, 2-flu
• dibenzofuran-3-ols and dibenzofuran-3-thiols can be used for the preparation of starting compounds of the formulae II and III: dibenzofuran-3-ol, dibenzofuran-3-thiol, 7-fluorodibenzofuran-3-ol, 7-chlorodibenzofuran-3-ol, 7-chlorodibenzofuran-3-thiol, 2,4,7-trichlorodibenzofuran-3-5-chlorodibenzofuran-3-ol, 6-chlorodibenzofuran-3-ol, 8-chlorodibenzofuran-3-ol, 5,7-dichlorobenzofuran-3-ol, 6,7-dichlorodibenzofuran-3-ol, 7,8-dichlorodibenzofuran-3-ol, 7-bromodibenzofuran-3-ol, 7-bromodibenzofuran-3-thio
• the novel active ingredients have a strong fungitoxic action on phytopathogenic fungi. They are particularly suitable for preventing and curing plant diseases caused by microorganisms such as Botrytis begonie, Botrytis cinerea, Plasmopara viticola, Monilia fructigena, Alternaria solani, Sclerotinia sclerotiorum, Piricularia oryzae, Pellicularia filamentosa, Erysiphe graminis, Erysiphe cichoriacearum, Chaetomium globosum, Sclerotinia cinerea, Aspergillus niger, Xanthomonas oryzae, and Xanthomonas citri.
• microorganisms such as Botrytis begonie, Botrytis cinerea, Plasmopara viticola, Monilia fructigena, Alternaria solani, Sclerotinia sclerotiorum, Piricularia ory
• the active ingredients according to the invention may simultaneously suppress the growth of two or more of the abovementioned fungi, and they are very well tolerated by plants. Some of the active ingredients have curative properties, i.e., the agents may also be applied after the plants have been infected by the pathogen, and success is still ensured.
• the fungicidal agents contain from 0.1 to 95, and preferably from 0.5 to 90, wt% of active ingredient.
• the application rates depend on the type of effect desired, and are from 0.1 to 5 kg of active ingredient per hectare.
• the agents according to the invention may also be mixed and applied with other active ingredients, e.g., herbicides, insecticides, growth regulators, other fungicides and fertilizers.
• active ingredients e.g., herbicides, insecticides, growth regulators, other fungicides and fertilizers.
• the spectrum of fungicidal action is in many cases increased; with a number of these fungicidal compositions, synergistic effects also occur; i.e., the fungicidal action of the combination product is greater than the effect of the individual components added together.
• the spectrum of action is particularly favorably influenced when the compounds according to the invention are mixed with the following fungicides: manganese N,N-ethylene-bis-dithiocarbamate, manganese zinc N,N-ethylenediamine-bis-dithiocarbamate, the ammonia complex of zinc N,N-ethylene-bis-dithiocarbamate and N,N'-polyethylene-bis(thiocarbamoyl)-disulfide, N-trichloromethylthiotetrahydrophthalimide, N-trichloromethylphthalimide, 5-ethoxy-3-trichloromethyl-1,2,3-thiadiazole, 2-methoxycarbonylaminobenzimidazole, 2-thiocyanomethylthiobenzothiazole, 1,4-dichloro-2,5-dimethoxybenzene, 2,3-dichloro-6-methyl-1,4-oxathiin-5-carboxylic acid anilide, 2-methyl-5,6-d
• the compounds according to the invention may also be combined with the following fungicides: dithiocarbamates and their derivatives, e.g. iron(III) dimethyldithiocarbamate, zinc dimethyldithiocarbamate, zinc N,N-ethylene-bis-dithiocarbamate, tetramethylthiuram disulfide, zinc N,N'-propylene-bis-dithiocarbamate, and the ammonia complex of zinc N,N'-propylene-bis-dithiocarbamate and N,N'-polypropylene-bis-(thiocarbamoyl)-disulfide; nitro derivatives, e.g.
• dodecylguanidine acetate 3-(2-(3,5-dimethyl-2-hydroxycyclohexyl)-2-hydroxyethyl)-glutarimide, hexachlorobenzene, N-dichlorofluoromethylthio-N',N'-dimethyl-N-phenyl-sulfuric acid diamide, 2,5-dimethyl-furan-3-carboxylic acid anilide, 2-methyl-benzoic acid anilide, 2-iodo-benzoic acid anilide, 1-(3,4-dichloroanilino)-1-formylamino-2,2,2-trichloroethane, 2,6-dimethyl-N-tridecylmorpholine and its salts, 2,6-dimethyl-N-cyclododecyl-morpholine and its salts, ⁇ -(2-chlorophenyl- ⁇ -(4-chlorophenyl)-5-pyrimidine-methanol, 1-(4
• the new active ingredients are applied for instance in the form of directly sprayable solutions, powders, suspensions (including high-percentage aqueous, oily or other suspensions or dispersions), emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering.
• the forms of application depend entirely on the purpose for which the agents are being used; at all events, they should ensure as fine a distribution of the active ingredient as possible.
• mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, further coal-tar oils, and oils of vegetable or animal origin
• aliphatic, cyclic and aromatic hydrocarbons such as benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives such as methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc.
• strongly polar solvents such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.
• Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions or wettable powders by adding water.
• emulsions, pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers.
• Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent, adherent, emulsifying or dispersing agent and possibly solvent or oil.
• surfactants are: alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid, naphthalenesulfonic acids, phenolsulfonic acids, alkylaryl sulfonates, alkyl sulfates, and alkyl sulfonates, alkali metal and alkaline earth metal salts of dibutylnaphthalenesulfonic acid, lauryl ether sulfate, fatty alcohol sulfates, alkali metal and alkaline earth metal salts of fatty acids, salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulf
• Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.
• Granules e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers.
• solid carriers are mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, Attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain flours, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.
• mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, Attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomace
• V. 20 parts by weight of compound no. 19 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene- ⁇ -sulfonic acid, 17 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, and triturated in a hammer mill.
• a spray liquor is obtained containing 0.1% by weight of the active ingredient.
• the agent used for comparison purposes was the prior art active ingredient tetramethylthiuram disulfide (Chem. Week, 111 (4), 39, 1972) known to be particularly suitable for combating Botrytis.
• Pimiento seedlings of the "Neusiedler Ideal Elite" variety were sprayed, after 4 to 5 leaves were well developed, to runoff with 0.025 wt% aqueous liquors containing (dry basis) 80% of active ingredient and 20% of sodium ligninsulfonate. After the sprayed-on layer had dried, the plants were sprinkled with a conidial suspension of the fungus Botrytis cinerea, and placed at 22° to 24° C. in a chamber of high humidity to obtain optimum conditions for promoting fungus growth. After 5 days, the disease had spread to such a great extent on the untreated plants that the necroses covered the major portion of the leaves.
• Leaves of pot-grown cucumber seedlings were sprayed with aqueous emulsions, the solids comprising 80% of active ingredient and 20% of emulsifier, and dusted, after the sprayed-on layer had dried, with spores of cucumber mildew (Erysiphe cichoriacearum).
• the plants were then placed in a greenhouse at from 20° to 22° C. and from 75 to 80% relative humidity. The extent of fungus development was determined after 10 days.
• the active ingredients are added, in amounts of 100, 50, 25, 12, 6 and 3 parts per million parts of solution, to a nutrient solution ideally suited for promoting the growth of the fungi Candida albicans and Oidium lactis.
• 10 ml of the mixture of nutrient solution and active ingredient was introduced into sterile test tubes and inoculated with one drop of a spore suspension containing 10 6 conidia or cells. After 120 hours' incubation, samples were taken from those tubes exhibiting no visible fungus growth and transferred to fungus nutrient media.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Wood Science & Technology (AREA)
• Environmental Sciences (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Zoology (AREA)
• Pest Control & Pesticides (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Plural Heterocyclic Compounds (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Furan Compounds (AREA)
• Saccharide Compounds (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=6123633

Family Applications (1)

Country Status (8)

Cited By (2)

Families Citing this family (5)

Citations (2)

Family Cites Families (3)

• 1981
  • 1981-01-30 DE DE19813103069 patent/DE3103069A1/de not_active Withdrawn
  • 1981-12-17 GR GR66824A patent/GR76955B/el unknown
• 1982
  • 1982-01-18 DE DE8282100301T patent/DE3260255D1/de not_active Expired
  • 1982-01-18 EP EP82100301A patent/EP0057362B1/fr not_active Expired
  • 1982-01-18 AT AT82100301T patent/ATE8046T1/de not_active IP Right Cessation
  • 1982-01-26 US US06/342,931 patent/US4376776A/en not_active Expired - Lifetime
  • 1982-01-29 JP JP57011935A patent/JPS57144278A/ja active Granted
  • 1982-01-29 IE IE199/82A patent/IE52438B1/en not_active IP Right Cessation
  • 1982-01-29 DK DK40182A patent/DK40182A/da not_active Application Discontinuation

Patent Citations (2)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events